Bipolar surgical morcellator

ABSTRACT

A device for morcellating tissue within a body cavity of a patient comprises a stationary tube ( 8 ) having a distal end portion, and a bipolar electrosurgical electrode assembly ( 13 ) located at the distal end of the tube. The electrosurgical electrode assembly ( 13 ) comprises first and second electrodes ( 14, 16 ) separated by an insulation member ( 15 ). When an electrosurgical cutting voltage is applied to the electrode assembly ( 13 ), and relative movement is initiated between the tube ( 8 ) and the tissue, a slug of resected tissue is formed within the tube such that it can be removed from the body cavity of the patient. The bipolar electrosurgical assembly ( 13 ) has a first circumferential region (A) and a second circumferential region (B), the first circumferential region (A) being longer than the second circumferential region (B), the bipolar electrosurgical assembly being adapted to cut tissue preferentially in the first circumferential region (A) as compared with the second circumferential region (B).

BACKGROUND OF THE INVENTION

This invention relates to a bipolar electrosurgical instrument for usein the bulk removal of tissue, as in a laparoscopic hysterectomy.

In a laparoscopic hysterectomy, the body of the uterus is resected fromthe stump or fundus, and then removed from the operative site. To enablethe uterus to be removed through a limited surgical opening, it isdesirable to morcellate it into relatively smaller pieces of tissue,which are easier to remove. Our pending patent application, published asWO05/112806 describes an electrosurgical morcellator for the bulkremoval of tissue. The present invention relates to an improvement tothis type of instrument.

A known problem with morcellating devices is their tendency to “coring”,in which the tip of the morcellator dives into the tissue in arelatively uncontrolled way. A preferred cutting technique is to use thedevice in a “peeling” action, in which the cutting instrument removestissue from the outside of an organ, rather like the peeling of an appleor orange. Peeling is preferred to coring for several reasons. A firstreason is that the tip of the morcellator is more visible to the surgeonif it is peeling around the outside of the tissue, as opposed to beingburied within the tissue as happens when the instrument is producing acore of tissue. Peeling produces a more continuous cut, and also a morecontinuous mass of uncut tissue. The more continuous cut means that theprocess can be completed more quickly, with the surgeon having tore-engage the tissue less often. Peeling from the outside of a solidorgan or mass of tissue leaves behind a more continuous mass of tissue,and less tissue fragments as compared with coring.

Published US patent application 2008/0039883 describes the problem withcoring, and provides a mechanical solution in the form of a protrusionsituated at the distal tip of the instrument. The present inventionattempts to provide an alternative solution, more suited to use with anelectrosurgical morcellator.

SUMMARY OF THE INVENTION

The present invention provides a device for morcellating tissue within abody cavity of a patient, the morcellating device comprising astationary tube having a distal end portion, the distal end portionincluding a stationary bipolar electrosurgical electrode assemblyincluding first and second electrodes located at the distal end of thetube and separated one from the other by an insulation member, thearrangement being such that, when an electrosurgical cutting voltage isapplied to the electrode assembly, tissue can be pulled against thedistal end of the tube to form a slug of resected tissue within thetube, the bipolar electrosurgical assembly having a firstcircumferential region and a second circumferential region, the firstand second electrodes being provided in the first circumferentialregion, the first circumferential region extending continuously aroundat least 50% of the tube, and the bipolar electrosurgical assembly beingadapted to cut tissue preferentially in the first circumferential regionas compared with the second circumferential region.

By providing an electrosurgical cutting assembly in which cutting isperformed preferentially in a first circumferential region, and eitherless effectively or not at all in a second circumferential region, thecutting instrument is unable to cut around the whole of the 360°circumference of the tube. This means that the cutting tip is lesslikely to be able to remove a core of tissue and become buried withinthe body of the organ being morcellated. With a section of the tissuebeing less easily cut, the morcellating instrument removes tissue at thesurface of the organ in a more controlled peeling action.

The second circumferential region should not be so great as tosubstantially affect the cutting capability of the instrument, and sothe first circumferential region extends around at least 50% of thecircumference of the tube. Other convenient arrangements have the secondcircumferential region constituting approximately 33%, 20% or even 10%of the circumference of the tube.

A convenient way of ensuring that the second circumferential region cutsless effectively than the first circumferential region is to ensure thatthe device is such that neither the first electrode nor the secondelectrode occupies the second circumferential region. In this way, theelectrosurgical cutting assembly is unable to perform an effective cutaround its entire circumference. Either the first (active) electrode orthe second (return) electrode can be provided in this way to disrupt thecutting action.

In one arrangement, an insulator occupies the second circumferentialregion. Thus, the first (active) electrode or the second (return)electrode extends continuously around the first circumferential region,but is replaced with an insulator in the second circumferential region.The electrosurgical cutting assembly is unable to cut effectively in theregion where the first electrode or the second electrode is replaced byan insulator, thereby providing the uncut portion of tissue which iseffective in promoting peeling and discouraging coring of tissue.

In an alternative arrangement, the second circumferential region is notmerely provided with an insulator instead of the first electrode or thesecond electrode, but instead comprises a third electrode spaced fromboth the first and second electrodes by one or more insulating sections.Preferably, the first, second and third electrodes each have separateleads connected thereto, such that the third electrode is capable ofbeing selectively switched in and out of common electrical potentialwith that of at least one of either the first and second electrodes. Inthis way, the third electrode can be selectively switched “on” so as toprovide a cutting action in collaboration with the first circumferentialregion, or alternatively switched “off” so as to act as an insulator aspreviously described. The instrument can, therefore, be controlled bythe user, either to peel tissue with the anti-coring system inoperation; or, if coring is required for some reason (or if the maximumcutting potential is required for a particularly difficult tissueextraction), the third electrode can be energised to provide cuttingaround the whole 360° circumference of the tube.

Conceivably, either the first electrode or the second electrode is splitinto three or more circumferential sections, each separated fromadjacent circumferential sections by means of insulators. In thisarrangement, the three or more circumferential sections preferably eachhave separate leads connected thereto, such that each circumferentialsection is capable of being switched into, and out of, common electricalpotential with other circumferential sections. The device preferablycarries a switch means capable of changing the circumferential sectionor sections that are switched out of common electric potential with theother circumferential sections. In this way, any one or more of thethree or more circumferential sections can be selectively switched tobecome insulated from the other sections, and hence become the secondcircumferential region described heretofore. This arrangement allows theuser of the instrument to select which circumferential region of thetube is to become less effective at cutting and hence provide theanti-coring effect. It is, therefore, not necessary for the user tore-orient the tube to accommodate a fixed anti-coring region, and theuser is able to change the anti-coring region depending on theorientation of the instrument. It is also possible for the user toincrease or decrease the number of sections that are insulated, so as tobe able to increase or decrease the anti-coring region as required.Conceivably, the switch means comprises a rotatable collar carried onthe device.

Alternatively, there is provided means for determining the orientationof the tube, and for activating the switch means so as to vary thecircumferential section or sections that are switched out of commonelectric potential with the other circumferential sections depending onthe orientation of the tube. In this way, the insulated section ismaintained in a predetermined orientation, regardless of which way thetube is oriented by the user. For example, it has been foundadvantageous to maintain the non-cutting section towards the outside ofthe body of tissue, on the “top” of the device as it is being used. Thiskeeps the morcellator towards the surface of the tissue, and prevents itfrom becoming buried within the tissue. By automatically orienting thenon-cutting section regardless of orientation, the user does not need tomake manual adjustments as the device is being used.

In one convenient arrangement, the tube is provided with a marker inalignment with the second circumferential region, to highlight itsposition to a user of the device. Thus the user always knows whichportion of the tube is provided with the anti-coring effect, regardlessof whether the circumferential region is fixed or changeable, manuallyor automatically.

In an alternative arrangement, the second circumferential region isprovided by covering the first or second electrode with anelectrically-insulating mask. This is in contrast to earlier describedarrangements in which the first electrode or the second electrode isinterrupted in the second circumferential region, either by aninsulating section or by a third electrode. In this alternativearrangement, the first electrode or the second electrode runscontinuously around the circumference of the tube, but is masked by theelectrically-insulating mask in the second circumferential region. Inone arrangement, the mask is selectively detachable from the firstelectrode or the second electrode. Alternatively, the mask isselectively deployable between a first position in which it obscures thefirst electrode or the second electrode, and a second position in whichit does not obscure the first electrode or the second electrode.Conveniently, the mask is selectively advanced and retracted between thefirst and second positions. Whichever arrangement is employed, the maskprevents effective cutting of tissue in the second circumferentialregion and provides the anti-coring effect previously described.

BRIEF DESCRIPTION OF THE DRAWINGS

The invention will now be described in more detail, by way of example,with reference to the drawings, in which:

FIG. 1 is a schematic side view, partly in section, of a morcellatingdevice constructed in accordance with the invention;

FIG. 2 is an enlarged view of a part of the device shown in FIG. 1,

FIG. 3 is an enlarged view of an alternative embodiment of amorcellating device constructed in accordance with the invention;

FIG. 4 is an enlarged view of a further embodiment of a morcellatingdevice constructed in accordance with the invention;

FIGS. 5A & 5B are enlarged views of different parts of a furtherembodiment of a morcellating device constructed in accordance with theinvention;

FIG. 6 is an enlarged view of yet another embodiment of a morcellatingdevice constructed in accordance with the invention;

FIG. 7 is an enlarged perspective view of a further embodiment of amorcellating device constructed in accordance with the invention; and

FIGS. 8 & 9 are enlarged views, partly in section, of the device of FIG.7.

DESCRIPTION OF PREFERRED EMBODIMENTS

Referring to FIG. 1, a morcellating system comprises a morcellatingdevice shown generally at 1, a tissue-pulling device shown generally at2, and an electrosurgical generator 3. The generator 3 is connected tothe morcellating device 1 by means of a cable 4, and to thetissue-pulling device 2 by means of a cable 5. The generator 3 iscontrolled by means of a footswitch 6.

As shown in FIGS. 1 and 2, the morcellating device 1 comprises a handle7 and a cylindrical tube 8. The cylindrical tube 8 is hollow, anddefines a lumen 9 therein. The proximal end of the tube 8 extends fromthe handle 7 as shown at 11, and the distal end of the tube is providedwith an electrosurgical electrode assembly 13. The electrosurgicalelectrode assembly 13 comprises an active tissue-cutting electrode 14,and an insulation member 15, both extending around the circumference ofthe tube 8. The insulation member 15 separates the active electrode 14from a return electrode 16, also located on the tube 8.

The active electrode 14 extends around the circumference of the tube 8,and is connected to one pole of the generator 3, via the cable 4. Thereturn electrode 16 is connected to the other pole of the generator 3,via the cable 4 and additional wiring (to be described later). In thisway, the electrodes 14 and 16 constitute the bipolar electrode assembly13, which, when energised by the generator 3, is capable of cuttingtissue coming into contact with the distal end of the tube 8.

The tissue-pulling device 2 comprises a tubular shaft 18, at theproximal end of which is a scissors-type handle mechanism 19, having afirst handle 20 and a second handle 21. The second handle 21 ispivotable with respect to the first handle 20, about a pivot pin 22.Pivoting of the second handle 21 causes longitudinal movement of a pushrod 23 extending through the shaft 18 to the distal end thereof.

At the distal end of the shaft 18 is a jaw assembly 24, with a first jawmember 25 and a second jaw member 26 movable between open and closedpositions by the movement of the push rod 23. The tissue-pulling device2 is manually translatable in a longitudinal manner within the lumen 9of the morcellating device 1. The jaw members 25 and 26 are electricallyconnected to the shaft 18, and the shaft is optionally electricallyconnected, via the cable 5 and a connector 28, with the generator 3. Theshaft 18 is connected to the same pole of the generator 3 as the returnelectrode 16.

The operation of the morcellating system is as follows. The tube 8 ofthe morcellating device 1 is inserted into the body of a patient,typically through a trocar (not shown), or optionally directly into anincision made in the body of the patient. The device 1 is brought intoposition adjacent to the tissue to be removed, which is typically aresected uterus in the case of a laparoscopic hysterectomy. Thetissue-pulling device 2 is then inserted through the lumen 9 of themorcellating device 1. The handle 21 is operated to open the jawassembly 24, and the tissue-pulling device 2 is manoeuvred so thattissue from the uterus is located between the jaw members 25 and 26. Thehandle 21 is then operated to close the jaw assembly 24, grasping tissuetherein.

The surgeon operates the footswitch 6 to operate the generator 3 so thatan electrosurgical cutting voltage is supplied between the activeelectrode 14 and the return electrode 16. As mentioned previously, thepush rod 23 and the jaw assembly 24 are also electrically connected tothe same pole of the generator 3 as the return electrode 16, and so boththe return electrode and the jaw assembly constitute a return. Withtissue firmly grasped in the jaw assembly 24, the tissue-pulling device2 is slowly withdrawn from the tube 8, pulling the tissue against thedistal end of the tube and against the active electrode 14. As thetissue contacts the active electrode 14, it is vaporised, allowing thetissue-pulling device 2 to be withdrawn further into the tube 8. In thisway, a cylindrical slug of tissue is formed in the tube 8, the tissuebeing withdrawn though the proximal end 10 of the morcellating device 1(which remains outside the body of the patient) for disposal.

The tissue-pulling device 2 can then be re-inserted into the tube 8 suchthat a further slug of tissue can be removed from the body of thepatient. By repeating this process, large quantities of tissue can beremoved from the patient in a relatively short time, such that theentire uterus can be removed, if necessary, while still employing alaparoscopic approach.

FIG. 2 shows the distal end of the tube 8 according to a firstembodiment of the invention, in which the active electrode 14 extendsaround the circumference of the tube 8 in a first circumferential regionA constituting more than 50% of the circumference of the tube, but doesnot extend into a second circumferential region B constituting less than50% of the circumference of the tube. In the second circumferentialregion B there is merely the exposed insulation member 15. The returnelectrode 16 extends completely around the tube 8 as shown. Leads 31 and32 respectively connect the electrodes 14 and 16 to the generator 3.When the electrosurgical cutting voltage is supplied between theelectrodes 14 and 16, and tissue is pulled against the electrodes by thetissue-pulling device 2, the tissue will be electrosurgically cut in theregion A, but remain unsevered in the region B. More and more tissue canbe pulled against the tube 8 by the retraction of the tissue-pullingdevice 2, and the result will be a peeling of tissue with a segment ofthe tissue remaining connected to the uterus adjacent to the region B.In this way, the tube 8 will remain towards the edge of the uterus,rather than being buried into the tissue to produce a coring action.

FIG. 3 shows an alternative distal arrangement in which the activeelectrode 14 extends continuously around the circumference of the tube8, but the return electrode 16 extends solely around region A, and isreplaced by an insulator 30 in region B. As the electrosurgical cuttingaction will only be effective where the active and return electrodes 14and 16 are in close proximity to one another, this arrangement willfunction in a similar fashion to that of the device of FIG. 2.

FIG. 4 shows a further arrangement, somewhat similar to that of FIG. 3in that the active electrode 14 extends around the circumference of thetube in a first circumferential region A, but does not extend into asecond circumferential region B. However, in the region B there isprovided a further active electrode 33 spaced from each circumferentialend of the electrode 14 by insulating spacers 34 and 35. The returnelectrode 16 extends completely around the circumference of the tube 8as shown. The lead 31 connects the active electrode 14 to the generator3, the lead 32 connects the return electrode 16 to the generator, and afurther lead 36 connects the further electrode 33 to the generator. Thefurther electrode 33 is connected to the generator 3 via a switchingdevice (not shown), the operation of which will now be described.

In a first situation, the switching device is set so that theelectrosurgical cutting voltage is supplied solely to the activeelectrode 14, such that the voltage is supplied between the electrodes14 and 16 in the region A, with no cutting action being created in theregion B. This is the anti-coring cutting action previously describedwith reference to FIGS. 2 and 3. However, there may be times when theuser of the morcellating device 1 needs to provide a cutting actioncompletely around the circumference of the tube 8, either because theuser wants to create a coring action, or because the nature of thetissue being treated means that the maximum cutting activity is needed.In this circumstance, the switching device is set so that theelectrosurgical cutting voltage is supplied to both active electrodes 14and 33 such that the voltage is supplied not only between the electrodes14 and 16 in the region A, but also between the electrodes 33 and 16 inthe region B. This means that the cutting action is available around thecomplete circumference of the tube 8, when desired. In an alternativearrangement, the further active electrode 33 is supplied with a lowervoltage than the electrosurgical cutting voltage, such that it is notcapable of cutting tissue but perhaps capable of coagulating tissue incombination with the return electrode 16. This will still provide theanti-coring action described previously, and may be useful where thetissue being dissected remains vascular, and where excessive bleeding isto be prevented.

FIGS. 5A and 5B show an even more sophisticated arrangement, in which aseries of active electrodes 14A, 14B, 14C, 14D etc. are disposed aroundthe circumference of the tube 8, each active electrode being separatedfrom circumferentially adjacent active electrodes by insulating spaces37. Each active electrode 14A to 14D is provided with its own lead (notshown), so that any combination of active electrodes can he energised ornot, depending on the circumstances. A rotatable collar 38 is providedon the tube 8, the collar having a series of contacts (not shown) on theinside thereof. Rotation of the collar 38 by the user of the deviceallows the user to select which active electrodes 14A to 14D areenergised. For example, rotation of the collar 38 to a first positionsets the contacts such that every electrode 14A to 14D is energised,such that the anti-coring system is deactivated and the device cutstissue around the entire circumference of the tube 8. Alternatively,rotating the collar 38 to a second position sets the contacts such thatone electrode 14A is not energised, whereas each of the remainingelectrodes 14B, 14C and 14D is energised. This inhibits cutting in theregion of the electrode 14A, and provides the anti-coring actiondescribed previously. Rotating the collar 38 to a further positionselects a different electrode 14B which is not energised, whereas eachof the other electrodes 14A, 14C and 14D is energised. In this way, theorientation of the tube 8 can be varied, and yet an active electrode canbe selected not to be energised, such that orientation of theanti-coring action remains constant with respect to the tissue beingtreated.

In an alternative arrangement, rotation of the collar 38 varies thenumber of active electrodes 14A to 14D that are not energised, ratherthan the position of the active electrode that is not energised. In thisway, the user can vary the extent of the anti-coring action provided bythe morcellating device 1.

FIG. 6 shows an alternative embodiment in which a collar 38 is alsoprovided, but in this embodiment the rotation of the collar causes acorresponding rotation of the electrosurgical assembly 13 at the distalend of the tube 8. The electrosurgical assembly 13 comprises a returnelectrode 16 which extends completely around the circumference of thetube 8, and an active electrode 14 which is interrupted in the region Bby means of an insulated section 30. The electrosurgical assembly 13 isconnected to the collar 38 by means of a sleeve 39, such that rotationof the collar causes a corresponding rotation of the electrosurgicalassembly 13. The insulated section 30 can, therefore, be rotated betweendifferent angular positions, hence varying the angular position of theanti-coring effect described previously.

FIGS. 7 to 9 show a different arrangement in which both the activeelectrode 14 and the return electrode 16 extend completely around thecircumference of the tube 8 at the distal end thereof. Anelectrically-insulating mask 41 is provided in a first circumferentialregion of the tube 8, so as to prevent the active electrode 14 fromengaging tissue in that region. The mask 41 prevents tissue cutting inthat region, and provides the anti-coring effect described previously.The mask 41 is typically an injection moulded polymer component, such asthe polymer-nylon material “Zytel”. In one arrangement, the mask 41 isdisposed within a compartment 42 at the end of the tube 8, and can beselectively advanced and retracted by the operation of an actuatingmechanism (not shown). When the mask 41 is advanced, it moves into aposition obscuring the active electrode 14 in the first circumferentialregion, thereby providing the anti-coring effect described previously.When the mask 41 is retracted into the compartment 42, it allows theactive electrode 14 to cut tissue around its entire circumference.

In an alternative arrangement, the mask 41 can be selectively attachedor detached from the tube 8, depending on whether the anti-coring effectis desired by the user of the morcellating device 1, or whether maximumcutting effectiveness is required.

It will he appreciated by those skilled in the art that many minormodifications and alternative constructions can be envisaged, withoutdeparting from the scope of the present invention. For example, the tube8 can be provided with a marker in alignment with the secondcircumferential region B, so as to highlight the position of that regionto a user of the device. Providing an effective electrosurgicaltissue-cutting assembly, in which a circumferential region of thecutting area is selectively inhibited, promotes the instrument toperform a peeling action on the tissue, and restricts the ability of theinstrument to become buried in the tissue in a coring manoeuvre.

1-15. (canceled)
 16. A device for morcellating tissue within a bodycavity of a patient, the morcellating device comprising a stationarytube having a distal end portion, the distal end portion including astationary bipolar electrosurgical electrode assembly including firstand second electrodes located at the distal end of the tube andseparated one from the other by an insulation member, the arrangementbeing such that, when an electrosurgical cutting voltage is applied tothe electrode assembly, tissue can be pulled against the distal end ofthe tube to form a slug of resected tissue within the tube, the bipolarelectrosurgical assembly having a first circumferential region and asecond circumferential region, the first circumferential regioncomprising first and second electrodes located at the distal end of thetube and being separated one from the other by at least one insulationmember, the first circumferential region extending continuously aroundat least 50% of the circumference of the tube, the bipolarelectrosurgical assembly being adapted to cut tissue preferentially inthe first circumferential region as compared with the secondcircumferential region.
 17. A morcellating device according to claim 16,wherein the device is such that only one of either the first electrodeor the second electrode occupies the second circumferential region, butnot both.
 18. A morcellating device according to claim 17, wherein aninsulator occupies a region of the second circumferential region.
 19. Amorcellating device according to claim 17, wherein the secondcircumferential region comprises a third electrode spaced from both thefirst and second electrodes by one or more insulating sections.
 20. Amorcellating device according to claim 19, wherein the first, second andthird electrodes each have separate leads connected thereto, such thatthe third electrode is capable of being selectively switched in and outof common electrical potential with that of at least one of either thefirst and second electrodes.
 21. A morcellating device according toclaim 16, wherein either the first electrode or the second electrode issplit into three or more circumferential sections, each separated fromadjacent circumferential sections by means of insulators.
 22. Amorcellating device according to claim 21, wherein the three or morecircumferential sections each has a separate lead connected thereto,such that each circumferential section is capable of being switched intoand out of common electrical potential with other circumferentialsections.
 23. A morcellating device according to claim 22, furthercomprising a switch capable of changing the circumferential section orsections that are switched out of common electric potential with theother circumferential sections.
 24. A morcellating device according toclaim 23, wherein the switch comprises a rotatable collar carried on thedevice.
 25. A morcellating device according to claim 23, furthercomprising means for determining the orientation of the tube, and foractivating the switch so as to vary the circumferential section orsections that are switched out of common electric potential with theother circumferential sections depending on the orientation of the tube.26. A morcellating device according to claim 16, wherein the tube isprovided with a marker in alignment with the second circumferentialregion, to highlight its position to a user of the device.
 27. Amorcellating device according to claim 16, wherein the secondcircumferential region is provided by covering the first or secondelectrode with an electrically-insulating mask.
 28. A morcellatingdevice according to claim 27, wherein the mask is selectively deployablebetween a first position in which it obscures the first electrode or thesecond electrode, and a second position in which it does not obscure thefirst electrode or the second electrode.
 29. A morcellating deviceaccording to claim 28, wherein the mask is selectively advanced andrefracted between the first and second positions.